Indole Alkaloids and Quassinoids from the Stems of Brucea mollis

被引:115
作者
Chen, Hui [1 ,2 ]
Bai, Jian [1 ,2 ]
Fang, Zhen-Feng [1 ,2 ]
Yu, Shi-Shan [1 ,2 ]
Ma, Shuang-Gang [1 ,2 ]
Xu, Song [1 ,2 ]
Li, Yong [1 ,2 ]
Qu, Jing [1 ,2 ]
Ren, Jin-Hong [1 ,2 ]
Li, Li [1 ,2 ]
Si, Yi-Kang [1 ,2 ]
Chen, Xiao-Guang [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Inst Mat Med, State Key Lab Bioact Subst & Funct Nat Med, Beijing 100050, Peoples R China
[2] Peking Union Med Coll, Beijing 100050, Peoples R China
来源
JOURNAL OF NATURAL PRODUCTS | 2011年 / 74卷 / 11期
关键词
CONSTITUENTS; GLYCOSIDES;
D O I
10.1021/np200712y
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Seven new indole alkaloids, bruceollines H-N (1-7), three new quassinoids, yadanziolides T-V (10-12), and four known analogues, bruceolline E (8), bruceolline F (9), bruceine D (13), and yadanziolide B (14), were isolated from an ethanol extract of the stems of Brucea mollis. The absolute configurations of compounds 2 and 5 were determined by comparison of their experimental and calculated ECD spectra. The absolute configuration of the known compound 9 was determined by using Mo-2(OAc)(4)-induced CD analysis for the first time. Compounds 10, 13, and 14 exhibited cytotoxic activities with IC50 values of 3.00-5.81 mu M.
引用
收藏
页码:2438 / 2445
页数:8
相关论文
共 23 条
[1]  
ABUZARGA MH, 1986, J NAT PROD, V49, P901
[2]  
[Anonymous], 2009, Curr. Bioact. Compd., DOI [10.2174/157340709787580900, DOI 10.2174/157340709787580900]
[3]   Determination of absolute configuration of acyclic 1,2-diols with Mo2(OAc)4.: 1.: Snatzke's method revisited [J].
Di Bari, L ;
Pescitelli, G ;
Pratelli, C ;
Pini, D ;
Salvadori, P .
JOURNAL OF ORGANIC CHEMISTRY, 2001, 66 (14) :4819-4825
[4]   Neolignans and Glycosides from the Stem Bark of Illicium difengpi [J].
Fang, Lei ;
Du, Dan ;
Ding, Guang-Zhi ;
Si, Yi-Kang ;
Yu, Shi-Shan ;
Liu, Yang ;
Wang, Wen-Jie ;
Ma, Shuang-Gang ;
Xu, Song ;
Qu, Jing ;
Wang, Jia-Ming ;
Liu, Yu-Xi .
JOURNAL OF NATURAL PRODUCTS, 2010, 73 (05) :818-824
[5]  
Frelek J, 1999, CURR ORG CHEM, V3, P117
[6]   Biologically active quassinoids and their chemistry: Potential leads for drug design [J].
Guo, Z ;
Vangapandu, S ;
Sindelar, RW ;
Walker, LA ;
Sindelar, RD .
CURRENT MEDICINAL CHEMISTRY, 2005, 12 (02) :173-190
[7]   C-18 AND C-19 QUASSINOIDS FROM EURYCOMA-LONGIFOLIA [J].
ITOKAWA, H ;
QIN, XR ;
MORITA, H ;
TAKEYA, K .
JOURNAL OF NATURAL PRODUCTS, 1993, 56 (10) :1766-1771
[8]   3-PRENYLINDOLES FROM MURRAYA-PANICULATA AND THEIR BIOGENETIC SIGNIFICANCE [J].
KINOSHITA, T ;
TATARA, S ;
HO, FC ;
SANKAWA, U .
PHYTOCHEMISTRY, 1989, 28 (01) :147-151
[9]   ANTI-TUMOR AGENTS .33. ISOLATION AND STRUCTURAL ELUCIDATION OF BRUCEOSIDE-A AND BRUCEOSIDE-B, NOVEL ANTI-LEUKEMIC QUASSINOID GLYCOSIDES, AND BRUCEIN-D AND BRUCEIN-E FROM BRUCEA-JAVA']JAVANICA [J].
LEE, KH ;
IMAKURA, Y ;
SUMIDA, Y ;
WU, RY ;
HALL, IH ;
HUANG, HC .
JOURNAL OF ORGANIC CHEMISTRY, 1979, 44 (13) :2180-2185
[10]   Pyrrolidinones from the Ascomycete Fungus Albonectria rigidiuscula [J].
Li, Jian ;
Liu, Shuchun ;
Niu, Shubin ;
Zhuang, Wenying ;
Che, Yongsheng .
JOURNAL OF NATURAL PRODUCTS, 2009, 72 (12) :2184-2187